These aren’t just any rings—they hold so much sentimental value. My engagement ring for obvious reasons but my wedding ring was my Nan’s wedding ring, a cherished gift she gave us on the day we got engaged.
I had never took my rings off since the day of our wedding so having them cut off left me in tears 😭
It is with a heavy heart that I write this blog post today, reflecting on the tragic and untimely death of Maeve Boothby-O’Neill, a young woman from the Myalgic Encephalomyelitis (ME) community. Maeve’s life was cut short at just 27 years old, not by the disease alone, but by the failings of a healthcare system that was ill-equipped to manage the complexities of her severe condition
As a wheelchair user, I understand the anxiety that comes with entrusting your mobility device to an airline, knowing that if something goes wrong, your entire trip could be jeopardised.
Join the ME Pyjama Party and Raise Awareness for Myalgic Encephalomyelitis!
Each year for ME Awareness Week in May and for Severe ME Day in August we wear PJs with the aim to make a significant impact in the lives of those living with Myalgic Encephalomyelitis (ME), also known as Chronic Fatigue Syndrome (CFS)
The National Disability Card is designed to provide proof of disability, making it easier for individuals to access various services, benefits, and discounts. It is a recognition tool that helps reduce the need for individuals to repeatedly prove their disability.
As Pride Month approaches each year, colourful displays of support, joy, and love for the LGBTQ+ community become widespread. However, within these celebrations, a notable portion of another community feels excluded and marginalised.
With a general election campaign now in full swing, we should be asking why it is still so hard for disabled people to run for office and what the next government will do about it.
I’m thrilled to invite you to a special event that aims to make a significant impact in the lives of those living with Myalgic Encephalomyelitis (ME), also known as Chronic Fatigue Syndrome (CFS).
We are all ready in Our Red PJs to help raise awareness of Myalgic Encephalomyelitis.
To join us all you need to do is take a pic in your PJs and post it to social media using #MEPJParty
Together, we can shed light on the challenges faced by those living with ME/CFS and advocate for greater understanding and support
As a passionate advocate for Myalgic Encephalomyelitis (ME) a complex and debilitating condition, I am deeply committed to raising awareness about the complexities and overwhelming impact of this condition.
